Nhân Viên Thẩm Định/ QV Officer

- To carry out the process validation: prepare protocol, follow- up the execution and report.
- To participate in cleaning validation:
- To participate in investigation and handling of deviations during process validation and cleaning validation, to follow- up the execution of corrective actions and report the results.
- To participate in preparation of SOPs related to validation/ qualification.
- To follow- up and update the product list and equipment database
- Any other duties related to validation/ qualification as assigned by Team leader.
- To participate in development and validation of the related analytical method, if needed
- To follow- up cleaning validation runs and take sample
- To support to carry out the qualification of production equipment and utilities.
- To support to carry out the analytical method validation: prepare protocol and utility.

- Minimum – 2 years experience in Validation at Pharmaceutical Factory
- Pharmacist, university degree

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Cập nhật gần nhất lúc: 2024-04-18 02:55:22